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Catalyst Database

Chronological list of catalyst events. Click "See Drug Details" to view detailed info in our AmpCard. Use the Sort options or search box below (e.g. "Phase 2") to filter the catalyst results.

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Drug | Disease (links)

Stage (next event)

Catalyst Date

CRVS

Phase 1

Soquelitinib (CPI-818) (ITK inhibitor)

Atopic dermatitis

Q2 2025

4/9/24- Ph1 trial initiated with initial clinical data in Q4 2024. Final data in early 2025. 11/12/24- Ph1 interim data in December 2024. 12/18/24- Lowest dose cohorts showed a favorable safety & efficacy profile. 1/13/25- Announced data from Cohort 2, full results in Q2 2025.

Data readout

KROS

Phase 2

KER-012 (cibotercept)

Pulmonary arterial hypertension and cardiovascular disorders

Q2 2025

TROPOS trial. 07/2023- Ph2 trial cleared. Presentation at PVRI '24 on Feb 2, 2024. 9/3/24- Closed screening, complete enrollment by end of Sep. 12/12/24- halted dosing in the 3.0 & 4.5 mg/kg treatment arms. 1/15/25- Halted dosing in all treatment arms. Patients to be monitored through the end-of-trial visits. Topline data from all treatment arms expected in Q2 2025.

Data readout

ALXO

Phase 2

Evorpacept (ALX148) + Keytruda

HNSCC (head and neck squamous cell carcinoma)

H1 2025

ASPEN-03 trial- dosed first patient on May 10, 2021. ASPEN-04 trial- first patient dosed on 7/28/21. 8/8/24 ASPEN 3 & ASPEN 4 trials topline results in H1 2025.

Data readout

VIR

Phase 2

VIR-3434 +/- VIR-2218 +/- PEG-IFNα

Chronic HBV infection (Hepatitis B virus)

H1 2025

PREVAIL platform: THRIVE & STRIVE trials. Initial data in H1 2025.

Data Readout

APRE

Phase 1

APR-1051

Advanced solid tumors

H1 2025

ACESOT-1051 trial. 3/11/24- IND cleared. 4/9/24- Poster presentation at AACR '24. 6/17/24- Dosed first patient. 10/23/24 Encouraging Ph1 preliminary results at EORTC-NCI-AACR. Updated safety/efficacy data in H1 2025.

Data readout

VSTM

PDUFA

Avutometinib (VS-6766) +/- Defactinib

recurrent KRAS mutant LGSOC (Low-Grade Serous Ovarian Cancer)

June 30, 2025

RAMP 201 & RAMP 301 studies. 5/24/24- Initiated rolling NDA submission. 10/17/24 Present mature dataset (RAMP 201) at IGCS '24. 10/31/24- Completed rolling NDA submission. 12/30/24- FDA accepted NDA under priority review with PDUFA target action date June 30, 2025. 2/20/25- Data at SGO '25 on March 14-17, 2025.

Approval decision

VYGR

Phase 1a

VY7523 (formerly VT- TAU01) [anti-tau antibody]

Alzheimer’s disease

H1 2025

3/27/24 File IND in H1 '24,Initiate Ph1a SAD in 2024 & Ph1b MAD in 2025. 8/6/24 Top-line safety and pharmacokinetic Ph1a SAD data expected in H1 2025. MAD PET imaging data in H2 2026.

Data readout

ANAB

Phase 3

Dostarlimab

Non-small cell lung carcinoma

H1 2025

COSTAR Lung trial. 8/16/23- Collab w/ GSK. Topline data in H1 2025.

Data readout

JAGX

Phase 2

Crofelemer powder

Microvillus Inclusion Disease (MVID) & SBS

H1 2025

8/8/23- IND accepted, proceed w/ Ph2. 11/01/23- Received US patent. 5/9/24- Submits CTA for Ph2 study in Italy and Germany. 12/18/24- Ph2 initiated. 1/22/25 - First patient dosed in investigator-initiated trial in UAE, PoC data in H1 2025.

Data Readout

KALA

Phase 2b

KPI-012

Persistent Corneal Epithelial Defect (PCED)

Q2 2025

CHASE study. 11/12/24- Enrollment ongoing. Topline data in Q2 2025.

Data Readout

Amp Volatility is calculated based off of options pricing with expiration after event.
Last Calculated: 03/13/20

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